WO1999053970A1 - Utilization of an autopolymerizing organosiloxane-based compound - Google Patents
Utilization of an autopolymerizing organosiloxane-based compound Download PDFInfo
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- WO1999053970A1 WO1999053970A1 PCT/DE1999/001215 DE9901215W WO9953970A1 WO 1999053970 A1 WO1999053970 A1 WO 1999053970A1 DE 9901215 W DE9901215 W DE 9901215W WO 9953970 A1 WO9953970 A1 WO 9953970A1
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- organosiloxane
- composition
- autopolymerizing
- intervertebral disc
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/14—Macromolecular materials
- A61L27/18—Macromolecular materials obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2430/00—Materials or treatment for tissue regeneration
- A61L2430/38—Materials or treatment for tissue regeneration for reconstruction of the spine, vertebrae or intervertebral discs
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S606/00—Surgery
- Y10S606/907—Composed of particular material or coated
- Y10S606/91—Polymer
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S623/00—Prosthesis, i.e. artificial body members, parts thereof, or aids and accessories therefor
- Y10S623/901—Method of manufacturing prosthetic device
Definitions
- a possible solution is to stiffen the movement segment with the risk of increased stress on the adjacent segments and the risk of connection instability.
- Another possibility is the artificial replacement of intervertebral discs, for example with the help of a hydrophilic material in a polyethylene network, which is implanted in the dry state.
- the intervertebral disc consists of an outer zone, the annulus fibrosus, with the so-called Sharpey fibers and a gelatinous parachondral inner zone, the nucleus pulposus.
- the autopolymerizing composition based on organosiloxane is preferably used for the production of implants only of the nucleus pulposus, while the anulos fibrosus remains unchanged. Since the composition used according to the invention is liquid or pasty, this composition can be introduced into the resulting cavity after removal of the gelatinous inner zone from the annulus fibrosus and is subject to autopolymerization there.
- composition polymerizes without additional heating to a permanently elastic silicone with complete filling of the cavity inside the annulus fibrosus, whereby a maximum area can be used for the load transfer, so that a uniform movement pattern is created.
- a permanently elastic silicone with complete filling of the cavity inside the annulus fibrosus, whereby a maximum area can be used for the load transfer, so that a uniform movement pattern is created.
- the organosiloxane-based composition used according to the invention is to be used in a sterilized state. Since such sterilization cannot usually be carried out by the user of the liquid or paste-like composition, it is expedient to sterilize the composition at the factory and to bring it to the market in sterile packaging.
- compositions used according to the invention must have the best possible biocompatibility in addition to the long-term durability. It was found that compositions based on polydimethylsiloxane produce silicones in autopolymerization which have both properties. As the intervertebral disc is exposed to considerable pressure loads, this result was surprising and unpredictable.
- the permanently elastic silicones obtained from polydimethylsiloxanes have no adverse effect on the tissue surrounding them, on the spread of the cell and normal cell division activity. No degenerative changes were found. Compositions based on linear polydimethylsiloxanes are particularly advantageous.
- the reaction time in the autopolymerization and the properties of the silicones obtained can be varied.
- phenyl radicals, ethyl groups or vinyl radicals can be incorporated instead of methyl groups, so that, for example, mixed methylphenyl, ethylmethyl or methylvinylsiloxanes are formed.
- the substituents can be arranged arbitrarily or as block copolymers.
- the end groups of the polydimethylsiloxanes are preferably trimethylsiloxy groups, but can at least partially also - 3 -
- Silanoi groups, vinyl groups or hydride end groups Silanoi groups, vinyl groups or hydride end groups.
- the viscosity of the linear polydimethsiloxanes can be controlled by chain termination groups, which is essential for the subject of the invention, since the compositions are said to be liquid to pasty when used.
- the compositions used according to the invention contain a catalyst.
- Known siloxane catalysts are amines, such as aminopropylsilane derivatives, and carboxylic acid salts of lead, tin and zinc, and organic salts of iron, cadmium, barium, antimony and zirconium. Tin octoates, laurates and oieates, and salts of dibutyl tin are particularly useful. However, those that are biologically compatible must be selected from the catalysts.
- Group VIII noble metal complexes such as platinum, rhodium and ruthenium, which in very small amounts, such as in concentrations as low as 1 to 2 ppm, catalyze the autopolymerization in acceptable polymerization times.
- platinum catalysts such as complex platinum olefins, can be used to catalyze an addition of Si-H end groups with olefins, such as vinyl-functional siloxanes.
- compositions which polymerize to permanently elastic silicones are therefore formed from mixtures of linear hydride-functional polydimethylsioxanes and linear vinyl-functional polydimethylsiloxanes in a mixture with a suitable catalyst, in particular a platinum catalyst such as chloroplatinic acid or another platinum compound.
- a suitable catalyst in particular a platinum catalyst such as chloroplatinic acid or another platinum compound.
- the catalyst is stored together with the vinyl-functional polydimethylsiloxanes in one package and the hydride-functional polydimethylsiloxane, optionally with a customary curing agent, optionally with the addition of vinyl-functional polydimethylsiloxane, but without a catalyst, in the second package.
- the proportions of the two polydimethylsiloxanes used depend on the desired properties of the permanently elastic silicone.
- Air humidity may also be used as a catalyst, but this is less important because of the required sterility of the composition in the application according to the invention.
- the average molecular weight (number average) of the compositions used according to the invention is in the range from 1,000 to 1,500,000, advantageously in the range from 50,000 to 100,000.
- the compositions used according to the invention can additionally contain customary fillers, such as finely divided silicas, such as fumed silica, such fillers having particle sizes of a maximum of 1 ⁇ m, for example in the range from 0.01 to 0.5 ⁇ m.
- suitable fillers are dehydrated silica gels, diatomaceous earth, finely divided titanium dioxide, aluminum oxide or zirconium oxide.
- customary auxiliaries can be incorporated into the compositions used according to the invention in the case of organosiloxane compositions, provided that these are biocompatible and do not impair the desired properties of the polymerized silicone, in particular the permanent elasticity and pressure resistance.
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Transplantation (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Dermatology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Materials For Medical Uses (AREA)
- Silicon Polymers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Prostheses (AREA)
Abstract
Description
Verwendung einer autopolymerisierenden Zusammensetzung auf Organosiloxanbasis Use of an organosiloxane-based autopolymerizing composition
Bereits ab dem dreißigsten Lebensjahr sind bei jedem Menschen degenerative Veränderungen der Bandscheibe nachzuweisen. Bei Bandscheibenvorfällen werden operative Eingriffe vorgenommen, die aber im Bereich der Lendenwirbelsäule von einer zum Teil hohen Mißerfolgsrate geprägt sind. Die Rate der Rezidivbandscheibenvorfäile und des sogenannten Failed Back Surgery Syndrom oder Postnucleotomiesyndroms ist relativ hoch. Dabei treten nach Nukleotomie Schmerzen auf, die häufig nach beschwerdefreiem Intervall in Erscheinung treten. Die zunehmende Degeneration des operierten Segments und die Degeneration der Bogengelenke werden als wesentliche Ursachen für ein sich verschlechterndes Langzeitergebnis angesehen. Dies bedeutet, daß eine der wichtigsten Ursachen der Beschwerden nach Bandscheibenoperationen die vermehrte Mobilität des Bewegungssegmentes darstellt. Eine mögliche Lösung ist die Versteifung des Bewegungssegmentes mit dem Risiko der vermehrten Belastung der angrenzenden Segmente und der Gefahr der Anschlußinstabilität. Eine andere Möglichkeit besteht in dem künstlichen Bandscheibenersatz beispielsweise mit Hilfe eines hydrophilen Materials in einem Polyethylennetz eingebunden, das im trockenen Zustand implantiert wird.From the age of thirty, degenerative changes in the intervertebral disc can be demonstrated in every person. In the case of herniated discs, surgical interventions are carried out, but these are characterized in part by the high failure rate in the area of the lumbar spine. The rate of recurrent herniated discs and the so-called failed back surgery syndrome or postnucleotomy syndrome is relatively high. Pain occurs after nucleotomy, which often occurs after a symptom-free interval. The increasing degeneration of the operated segment and the degeneration of the arch joints are considered to be the main causes of a worsening long-term result. This means that one of the most important causes of complaints after intervertebral disc surgery is the increased mobility of the movement segment. A possible solution is to stiffen the movement segment with the risk of increased stress on the adjacent segments and the risk of connection instability. Another possibility is the artificial replacement of intervertebral discs, for example with the help of a hydrophilic material in a polyethylene network, which is implanted in the dry state.
Versuche mit einem Wirbelsäulenmodell ergaben, daß eine wesentliche Ursache für ein sich verschlechterndes Langzeitergebnis nach Bandscheibenoperationen die vermehrte Mobilität des Bewegungssegmentes ist. Die der Erfindung zugrundeliegende Aufgabe bestand somit darin, Bandscheibenimplantate zu bekommen, die das physiologische Bewegungsausmaß der Bandscheibe so gut wie möglich wiederherstellen. Diese Aufgabe wird erfindungsgemäß gelöst, indem man eine flüssige oder pastenartige, bei Umgebungstemperatur zu dauerelastischem Silicon autopolymerisierende Zusammensetzung auf Organosiloxanbasis zur Herstellung von Bandscheibenimplantaten verwendet.Experiments with a spine model have shown that a major cause of a deteriorating long-term result after intervertebral disc surgery is the increased mobility of the movement segment. The object underlying the invention was therefore to obtain intervertebral disc implants that restore the physiological range of movement of the intervertebral disc as well as possible. This object is achieved according to the invention by using a liquid or paste-like composition based on organosiloxane that is autopolymerizing at room temperature to form permanently elastic silicone for the production of intervertebral disc implants.
Die Bandscheibe besteht aus einer Außenzone, dem Anulus fibrosus, mit den sogenannten Sharpeyschen Fasern und einer gallertartigen parachondralen Innenzone, dem Nucleus pulposus. Erfindungsgemäß wird die autopolymerisierende Zusammenetzung auf Organosiloxanbasis vorzugsweise zur Herstellung von Implantaten lediglich des Nucleus pulposus verwendet, während der Anulos fibrosus unverändert erhalten bleibt. Da die erfindungsgemäß verwendete Zusammensetzung flüssig oder pastenartig ist, kann diese Zusammensetzung nach Entfernung der gallertartigen Innenzone aus dem Anulus fibrosus in den entstandenen Hohlraum eingeführt werden und unterliegt dort der Autopolymerisation. Der Anulus fibrosus - 2 -The intervertebral disc consists of an outer zone, the annulus fibrosus, with the so-called Sharpey fibers and a gelatinous parachondral inner zone, the nucleus pulposus. According to the invention, the autopolymerizing composition based on organosiloxane is preferably used for the production of implants only of the nucleus pulposus, while the anulos fibrosus remains unchanged. Since the composition used according to the invention is liquid or pasty, this composition can be introduced into the resulting cavity after removal of the gelatinous inner zone from the annulus fibrosus and is subject to autopolymerization there. The annulus fibrosus - 2 -
dient also dabei einerseits dazu, den Abstand der Wirbelsegmente zu halten, andererseits aber gleichzeitig als Form für die flüssige oder pastenförmige Zusammensetzung nach der Erfindung, die in den Innenraum dieser Form eingespritzt wird. Hierzu genügt ein endoskopisch minimal invasiver Zugang zur Bandscheibe über den retroperitonealen Raum von ventral oder über den standardisierten Zugang von dorsal. Nach dem Ausräumen des Nucleus pulposus und Einbringen der hydrophoben Zusammensetzung auf Organosiloxanbasis nach der Erfindung kann der Anulus fibrosus anschließend verschlossen werden. Die Zusammensetzung polymerisiert ohne zusätzliche Erwärmung zu einem dauerelastischen Silicon unter kompletter Ausfüllung des Hohlraumes innerhalb des Anulus fibrosus, wobei eine maximale Fläche für die Lastübertragung genutzt werden kann, so daß ein gleichmäßiges Bewegungsbild entsteht. Mit der Erfindung kann daher die segmentale Stabilität des nukleotomierten Bandscheibensegmentes wiederhergestellt werden.thus serves on the one hand to keep the distance between the vertebral segments, but on the other hand at the same time as a form for the liquid or pasty composition according to the invention which is injected into the interior of this form. All that is required is an endoscopically minimally invasive access to the intervertebral disc via the retroperitoneal space from the ventral or via the standardized access from the dorsal. After the nucleus pulposus has been cleared out and the hydrophobic organosiloxane-based composition according to the invention has been introduced, the annulus fibrosus can then be closed. The composition polymerizes without additional heating to a permanently elastic silicone with complete filling of the cavity inside the annulus fibrosus, whereby a maximum area can be used for the load transfer, so that a uniform movement pattern is created. With the invention, therefore, the segmental stability of the nucleotomized intervertebral disc segment can be restored.
Die erfindungsgemäß verwendete Zusammensetzung auf Organosiloxanbasis ist in sterilisiertem Zustand zu verwenden. Da eine solche Sterilisierung im Regelfall nicht vom Verwender der flüssigen oder pastenförmigen Zusammensetzung durchgeführt werden kann, ist es zweckmäßig, die Zusammensetzung werkseitig zu sterilisieren und in einer innensterilen Verpackung in den Handel zu bringen.The organosiloxane-based composition used according to the invention is to be used in a sterilized state. Since such sterilization cannot usually be carried out by the user of the liquid or paste-like composition, it is expedient to sterilize the composition at the factory and to bring it to the market in sterile packaging.
Die erfindungsgemäß verwendeten Zusammensetzungen müssen neben möglichst hoher Dauerbelastungsfähigkeit eine möglichst gute Biokompatibilität haben. Es zeigte sich, daß Zusammensetzungen auf Polydimethylsiloxanbasis bei der Autopolymerisation Silicone ergeben, die beide Eigenschaften besitzen. Da die Bandscheibe erheblichen Druckbelastungen ausgesetzt ist, war dieses Ergebnis überraschend und nicht vorhersehbar. Die aus Polydime- thylsiloxanen erhaltenen dauerelastischen Silicone haben keinen nachteiligen Einfluß auf das sie umgebende Gewebe, auf die Zeliausbreitung und normale Zellteilungsaktivität. Degenerative Veränderungen wurden nicht festgestellt. Insbesondere sind Zusammensetzungen auf der Basis linearer Polydimethylsiloxane von Vorteil.The compositions used according to the invention must have the best possible biocompatibility in addition to the long-term durability. It was found that compositions based on polydimethylsiloxane produce silicones in autopolymerization which have both properties. As the intervertebral disc is exposed to considerable pressure loads, this result was surprising and unpredictable. The permanently elastic silicones obtained from polydimethylsiloxanes have no adverse effect on the tissue surrounding them, on the spread of the cell and normal cell division activity. No degenerative changes were found. Compositions based on linear polydimethylsiloxanes are particularly advantageous.
Durch Copolymerisation der Methylsiioxane mit anders substituierten Siloxanen können die Reaktionsdauer bei der Autopolymerisation und die Eigenschaften der erhaltenen Silicone variiert werden. Beispielsweise können statt Methylgruppen Phenylreste, Ethylgruppen oder Vinylreste eingebaut werden, so daß beispielsweise gemischte Methylphenyl-, Ethylmethyl- oder Methylvinylsiloxane entstehen. Bei solchen Copolymerisaten können die Substituenten willkürlich oder als Blockcopolymere angeordnet werden. Die Endgruppen der Polydimethylsiloxane sind vorzugsweise Trimethylsiloxygruppen, können aber wenigstens teilweise auch - 3 -By copolymerizing the methylsiioxanes with other substituted siloxanes, the reaction time in the autopolymerization and the properties of the silicones obtained can be varied. For example, phenyl radicals, ethyl groups or vinyl radicals can be incorporated instead of methyl groups, so that, for example, mixed methylphenyl, ethylmethyl or methylvinylsiloxanes are formed. In such copolymers, the substituents can be arranged arbitrarily or as block copolymers. The end groups of the polydimethylsiloxanes are preferably trimethylsiloxy groups, but can at least partially also - 3 -
Silanoigruppen, Vinylgruppen oder Hydridendgruppen sein. Die Viskosität der linearen Polydimethγlsiloxane kann durch Kettenabbruchgruppen gesteuert werden, was für den Erfindungsgegenstand wesentlich ist, da die Zusammensetzungen bei der Verwendung flüssig bis pastenartig sein sollen.Silanoi groups, vinyl groups or hydride end groups. The viscosity of the linear polydimethsiloxanes can be controlled by chain termination groups, which is essential for the subject of the invention, since the compositions are said to be liquid to pasty when used.
Um bei Umgebungstemperatur autopolymerisierend zu sein, enthalten die erfindungsgemäß verwendeten Zusammensetzungen einen Katalysator. Bekannte Siloxankatalysatoren sind Amine, wie Aminopropylsilanderivate, und Carbonsäuresalze von Blei, Zinn und Zink sowie organische Salze von Eisen, Cadmium, Barium, Antimon und Zirkonium. Zinnoctoate, -laurate und -oieate sowie Salze von Dibutylzinn sind besonders brauchbar. Unter den Katalysatoren müssen allerdings solche ausgewählt werden, die biologisch verträglich sind. Hierzu gehören insbesondere additionskatalysierende Edelmetallkomplexe der Gruppe VIII, wie von Platin, Rhodium und Ruthenium, die in sehr kleinen Mengen, wie in Konzentrationen so niedrig wie 1 bis 2 ppm, die Autopolymerisation in annehmbaren Polymerisationszeiten katalysieren. Insbesondere sind Platinkatalγsatoren, wie Platin-Olef inkomplexe, brauchbar, eine Addition von Si-H-Endgruppen mit Olefinen, wie vinylfunktionellen Siloxanen zu katalysieren. Bevorzugte Zusammensetzungen, die zu dauereiastischen Siliconen polymerisieren, werden daher von Gemischen linearer hydridfunktioneller Polydimethylsiioxane und linearer vinylfunktioneller Polydimethylsiloxane im Gemisch mit einem geeigneten Katalysator, insbesondere einem Platinkatalysator, wie Chlorplatinsäure oder einer anderen Platinverbindung, gebildet. Um eine vorzeitige Polyaddition zu verhindern, werden solche Zusammensetzungen in zwei getrennten Packungen gelagert und erst unmittelbar vor der Verwendung miteinander vereinigt. Gewöhnlich wird der Katalysator zusammen mit den vinylfunktionellen Polydimethylsiloxanen in einer Verpackung und das hydridfunktionelle Polydimethylsiloxan, gegebenenfalls mit einem üblichen Härtungsmittel, gegebenenfalls unter Zugabe von vinylfunktionellem Polydimethylsiloxan, aber ohne Katalysator, in der zweiten Verpackung aufbewahrt. Die verwendeten Mengenverhältnisse der beiden Polydimethylsiloxane hängen von den erwünschten Eigenschaften des dauerelastischen Silicons ab.In order to be autopolymerizing at ambient temperature, the compositions used according to the invention contain a catalyst. Known siloxane catalysts are amines, such as aminopropylsilane derivatives, and carboxylic acid salts of lead, tin and zinc, and organic salts of iron, cadmium, barium, antimony and zirconium. Tin octoates, laurates and oieates, and salts of dibutyl tin are particularly useful. However, those that are biologically compatible must be selected from the catalysts. These include, in particular, addition-catalyzing Group VIII noble metal complexes, such as platinum, rhodium and ruthenium, which in very small amounts, such as in concentrations as low as 1 to 2 ppm, catalyze the autopolymerization in acceptable polymerization times. In particular, platinum catalysts, such as complex platinum olefins, can be used to catalyze an addition of Si-H end groups with olefins, such as vinyl-functional siloxanes. Preferred compositions which polymerize to permanently elastic silicones are therefore formed from mixtures of linear hydride-functional polydimethylsioxanes and linear vinyl-functional polydimethylsiloxanes in a mixture with a suitable catalyst, in particular a platinum catalyst such as chloroplatinic acid or another platinum compound. In order to prevent premature polyaddition, such compositions are stored in two separate packages and are only combined with one another immediately before use. Usually the catalyst is stored together with the vinyl-functional polydimethylsiloxanes in one package and the hydride-functional polydimethylsiloxane, optionally with a customary curing agent, optionally with the addition of vinyl-functional polydimethylsiloxane, but without a catalyst, in the second package. The proportions of the two polydimethylsiloxanes used depend on the desired properties of the permanently elastic silicone.
Gegebenenfalls kommt als Katalysator auch Luftfeuchtigkeit in Betracht, doch ist dies wegen der erforderlichen Sterilität der Zusammensetzung bei der erfindungsgemäßen Anwendung weniger bedeutsam.Air humidity may also be used as a catalyst, but this is less important because of the required sterility of the composition in the application according to the invention.
Das mittlere Molekulargewicht (Zahlenmittel) der erfindungsgemäß verwendeten Zusammensetzungen liegt im Bereich von 1000 bis 1 50 000, zweckmäßig im Bereich von 50 000 bis 100 000. Die erfindungsgemäß verwendeten Zusammensetzungen können zusätzlich übliche Füllstoffe, wie feinteilige Kieselsäuren, wie Rauchkieseisäure, enthalten, wobei solche Füllstoffe Teilchengrößen von maxial 1 μm, wie beispielsweise im Bereich von 0,01 bis 0,5 μm, haben sollten. Andere in Betracht kommende Füllstoffe sind dehydrierte Kieselgele, Diatomeenerde, feinteiliges Titandioxid, Aluminiumoxid oder Zirkonoxid. Im übrigen können in die erfindungsgemäß verwendeten Zusammensetzungen bei Organosiloxanmassen übliche Hilfsstoffe eingearbeitet werden, sofern diese biokompatibel sind und die erwünschten Eigenschaften des auspolymerisiserten Silicons, insbesondere die Dauerelastizität und Druckbeständigkeit, nicht beeinträchtigen. The average molecular weight (number average) of the compositions used according to the invention is in the range from 1,000 to 1,500,000, advantageously in the range from 50,000 to 100,000. The compositions used according to the invention can additionally contain customary fillers, such as finely divided silicas, such as fumed silica, such fillers having particle sizes of a maximum of 1 μm, for example in the range from 0.01 to 0.5 μm. Other suitable fillers are dehydrated silica gels, diatomaceous earth, finely divided titanium dioxide, aluminum oxide or zirconium oxide. Otherwise, customary auxiliaries can be incorporated into the compositions used according to the invention in the case of organosiloxane compositions, provided that these are biocompatible and do not impair the desired properties of the polymerized silicone, in particular the permanent elasticity and pressure resistance.
Claims
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP99927712A EP1071484B1 (en) | 1998-04-22 | 1999-04-21 | Utilization of an autopolymerizing organosiloxane-based compound |
| AU44976/99A AU4497699A (en) | 1998-04-22 | 1999-04-21 | Utilization of an autopolymerizing organosiloxane-based compound |
| DE59900296T DE59900296D1 (en) | 1998-04-22 | 1999-04-21 | USE OF AN ORGANOSILOXANE-BASED AUTOPOLYMERIZING COMPOSITION |
| CA002329329A CA2329329C (en) | 1998-04-22 | 1999-04-21 | Intervertebral disc implants produced from an autopolymerizing organosiloxane-based composition |
| US09/673,865 US6520992B1 (en) | 1998-04-22 | 1999-04-21 | Utilization of an autopolymerizing organosiloxane-based compound |
| JP2000544373A JP4550277B2 (en) | 1998-04-22 | 1999-04-21 | Intervertebral disc grafts using organosiloxane-based self-polymerizing compounds |
| AT99927712T ATE206315T1 (en) | 1998-04-22 | 1999-04-21 | USE OF AN ORGANOSILOXANE-BASED AUTOPOLYMERIZING COMPOSITION |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19817698.8 | 1998-04-22 | ||
| DE19817698A DE19817698A1 (en) | 1998-04-22 | 1998-04-22 | Composition used for flat disk implant, especially nucleus pulposus implant |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1999053970A1 true WO1999053970A1 (en) | 1999-10-28 |
Family
ID=7865262
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/DE1999/001215 Ceased WO1999053970A1 (en) | 1998-04-22 | 1999-04-21 | Utilization of an autopolymerizing organosiloxane-based compound |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US6520992B1 (en) |
| EP (1) | EP1071484B1 (en) |
| JP (1) | JP4550277B2 (en) |
| AT (1) | ATE206315T1 (en) |
| AU (1) | AU4497699A (en) |
| CA (1) | CA2329329C (en) |
| DE (2) | DE19817698A1 (en) |
| ES (1) | ES2165737T3 (en) |
| WO (1) | WO1999053970A1 (en) |
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| US8197545B2 (en) | 2005-10-27 | 2012-06-12 | Depuy Spine, Inc. | Nucleus augmentation delivery device and technique |
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| JP2002505592A (en) | 1996-11-15 | 2002-02-19 | アドバンスト バイオ サーフェイシズ,インコーポレイティド | Biomaterial systems used to repair tissue in situ |
| ES2491866T3 (en) | 1999-11-15 | 2014-09-08 | Piramal Healthcare (Canada) Limited | Temperature-controlled, pH-dependent, self-gelling aqueous biopolymer solution |
| US6899716B2 (en) * | 2000-02-16 | 2005-05-31 | Trans1, Inc. | Method and apparatus for spinal augmentation |
| US7744599B2 (en) * | 2000-02-16 | 2010-06-29 | Trans1 Inc. | Articulating spinal implant |
| BR0112109A (en) | 2000-06-29 | 2007-05-29 | Biosyntech Canada Inc | composition and method for the correction and regeneration of cartilage and other tissues |
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- 1999-04-21 ES ES99927712T patent/ES2165737T3/en not_active Expired - Lifetime
- 1999-04-21 EP EP99927712A patent/EP1071484B1/en not_active Expired - Lifetime
- 1999-04-21 CA CA002329329A patent/CA2329329C/en not_active Expired - Lifetime
- 1999-04-21 DE DE59900296T patent/DE59900296D1/en not_active Expired - Lifetime
- 1999-04-21 US US09/673,865 patent/US6520992B1/en not_active Expired - Lifetime
- 1999-04-21 AU AU44976/99A patent/AU4497699A/en not_active Abandoned
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| US8197545B2 (en) | 2005-10-27 | 2012-06-12 | Depuy Spine, Inc. | Nucleus augmentation delivery device and technique |
| US9162041B2 (en) | 2005-10-27 | 2015-10-20 | DePuy Synthes Products, Inc. | Nucleus augmentation delivery device and technique |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2329329C (en) | 2008-12-02 |
| DE19817698A1 (en) | 1999-10-28 |
| CA2329329A1 (en) | 1999-10-28 |
| EP1071484B1 (en) | 2001-10-04 |
| JP2002512089A (en) | 2002-04-23 |
| JP4550277B2 (en) | 2010-09-22 |
| ES2165737T3 (en) | 2002-03-16 |
| EP1071484A1 (en) | 2001-01-31 |
| ATE206315T1 (en) | 2001-10-15 |
| AU4497699A (en) | 1999-11-08 |
| US6520992B1 (en) | 2003-02-18 |
| DE59900296D1 (en) | 2001-11-08 |
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